Drug recall
Pooled Cryoprecipitated AHF
FDA recall event 88901 · Class II · American National Red Cross, Penn Jersey Region
Key facts
| Event ID | 88901 |
|---|---|
| Recall numbers | B-0046-2022, B-0047-2022 |
| Recalling firm | American National Red Cross, Penn Jersey Region |
| Product type | Biologics |
| Products | Pooled Cryoprecipitated AHF, Red Blood Cells, Leukocytes Reduced, Irradiated |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Blood Products, in which West Nile Virus Testing was performed incorrectly, were distributed. |
| Initiation date | Aug 25, 2021 |
| Report date | Nov 24, 2021 |
| Termination date | Nov 18, 2021 |
| City | Philadelphia |
| State | PA |
| Country | United States |
| FEI number | 2573021 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: